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常染色体显性遗传性肢带型肌营养不良的临床与遗传学研究

Clinical and genetic investigation in autosomal dominant limb-girdle muscular dystrophy.

作者信息

Gilchrist J M, Pericak-Vance M, Silverman L, Roses A D

机构信息

Division of Neurology, Duke University Medical Center, Durham, NC.

出版信息

Neurology. 1988 Jan;38(1):5-9. doi: 10.1212/wnl.38.1.5.

Abstract

Limb-girdle muscular dystrophy is a syndrome of progressive myopathic weakness affecting shoulder and hip girdle and proximal arm and leg muscles. The disease occurs either sporadically or inherited as an autosomal recessive trait. Autosomal dominant inheritance is rare. We report a large family with apparent autosomal dominant inheritance. Sixteen members were affected with a disease characterized by proximal weakness, leg greater than arm, onset in the third decade, elevated CK and CK MB levels, and myopathic EMGs and muscle biopsies. Linkage analysis revealed no conclusive linkage.

摘要

肢带型肌营养不良是一种进行性肌病性肌无力综合征,影响肩胛带和骨盆带以及近端上肢和下肢肌肉。该疾病可散发出现,也可作为常染色体隐性性状遗传。常染色体显性遗传较为罕见。我们报告了一个具有明显常染色体显性遗传特征的大家族。16名成员受一种疾病影响,其特征为近端肌无力,腿部比手臂更明显,发病于第三个十年,肌酸激酶(CK)和肌酸激酶同工酶(CK MB)水平升高,以及肌病性肌电图和肌肉活检结果。连锁分析未发现确凿的连锁关系。

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